钐
钙钛矿(结构)
钝化
材料科学
热稳定性
掺杂剂
氧化还原
化学工程
化学计量学
无机化学
兴奋剂
化学
纳米技术
物理化学
冶金
光电子学
工程类
图层(电子)
作者
Yang Yang,Dongwei Han,Ying Yang,Siwei Yi,Quan Yuan,Dong‐Ying Zhou,Lai Feng
出处
期刊:APL Materials
[American Institute of Physics]
日期:2020-07-01
卷期号:8 (7)
被引量:20
摘要
All-inorganic (CsPbX3) perovskites by replacing the volatile organic components with cesium cations allow extending the long-term thermal stability of perovskite solar cells (PeSCs) vs their organic–inorganic hybrid counterparts. However, the stability of α-CsPbI3 and α-CsPbI2Br still remains to be improved. In this work, we incorporate redox-inactive samarium acetylacetonate [Sm(acac)3] into CsPbI2Br to fabricate CsPbI2Br perovskite thin films. It is evidenced that Sm3+ not only partially substitute the Pb2+ sites to yield slightly contracted perovskite lattice but also modulate the perovskite growth and passivate the NiOx/CsPbI2Br interface. As a result, CsPbI2Br PeSCs based on stoichiometric and optimal Sm(acac)3 doping (0.15 mol. %) of CsPbI2Br show excellent photovoltaic metrics with a champion power conversion efficiency (PCE) of 12.86%. Moreover, the CsPbI2Br PeSCs exhibit enhanced thermal stability upon incorporation of Sm(acac)3, which retains 90% of their original PCE under heating at 85 °C for 200 h.
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